The molecular lesion is a C-to-T missense mutation (973C-T) in codon 325 in exon 3. This is predicted to alter amino acid 325 from an aspartic acid to an asparagine (D325N) in the encoded protein. (J:237905)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count